rs786202033

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;C)	6.7	CDH1-based gastric cancer risk
(C;C)	0	common in clinvar

Make rs786202033(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

68823461

Gene

CDH1

is a	snp
is	mentioned by
dbSNP	rs786202033
dbSNP (classic)	rs786202033
ClinGen	rs786202033
ebi	rs786202033
HLI	rs786202033
Exac	rs786202033
Gnomad	rs786202033
Varsome	rs786202033
LitVar	rs786202033
Map	rs786202033
PheGenI	rs786202033
Biobank	rs786202033
1000 genomes	rs786202033
hgdp	rs786202033
ensembl	rs786202033
geneview	rs786202033
scholar	rs786202033
google	rs786202033
pharmgkb	rs786202033
gwascentral	rs786202033
openSNP	rs786202033
23andMe	rs786202033
SNPshot	rs786202033
SNPdbe	rs786202033
MSV3d	rs786202033
GWAS Ctlg	rs786202033

Max Magnitude

6.7

Also known as c.1999delC, the minor allele is considered a pathogenic rare mutation for hereditary diffuse gastric cancer in ClinVar.

ClinVar
Risk	rs786202033(-;-)
Alt	rs786202033(-;-)
Reference	Rs786202033(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	CDH1
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000016.9:g.68857364delC
CLNSRC
CLNACC	RCV000164640.1, RCV000376724.1,